Pettersson U - Search Results

1

Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies.

Wadelius C, Blombäck M, Pettersson U. Wadelius C, et al. Among authors: pettersson u. Hum Genet. 1988 Dec;81(1):13-7. doi: 10.1007/BF00283721. Hum Genet. 1988. PMID: 2848757

2

Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Wadelius C, Fagerholm P, Pettersson U, Annerén G. Wadelius C, et al. Among authors: pettersson u. Am J Hum Genet. 1989 Feb;44(2):241-7. Am J Hum Genet. 1989. PMID: 2912070 Free PMC article.

3

Hemophilia B in a 46,XX female probably caused by non-random X inactivation.

Wadelius C, Lindstedt M, Pigg M, Egberg N, Pettersson U, Anvret M. Wadelius C, et al. Among authors: pettersson u. Clin Genet. 1993 Jan;43(1):1-4. doi: 10.1111/j.1399-0004.1993.tb04415.x. Clin Genet. 1993. PMID: 8096443

4

Linkage mapping of a severe X-linked mental retardation syndrome.

Malmgren H, Sundvall M, Dahl N, Gustavson KH, Annerén G, Wadelius C, Steén-Bondeson ML, Pettersson U. Malmgren H, et al. Among authors: pettersson u. Am J Hum Genet. 1993 Jun;52(6):1046-52. Am J Hum Genet. 1993. PMID: 8503440 Free PMC article.

5

Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome.

Dahl N, Hammarström-Heeroma K, Goonewardena P, Wadelius C, Gustavson KH, Holmgren G, van Ommen GJ, Pettersson U. Dahl N, et al. Among authors: pettersson u. Hum Genet. 1989 Jun;82(3):216-8. doi: 10.1007/BF00291157. Hum Genet. 1989. PMID: 2567272

6

Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.

Ahlbom BE, Goetz P, Korenberg JR, Pettersson U, Seemanova E, Wadelius C, Zech L, Annerén G. Ahlbom BE, et al. Among authors: pettersson u. Am J Med Genet. 1996 Jun 28;63(4):566-72. doi: 10.1002/(SICI)1096-8628(19960628)63:4<566::AID-AJMG10>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826436

7

Evaluation of DNA-based diagnosis for haemophilia A.

Wadelius C, Blombäck M, Goonewardena P, Anvret M, Lindstedt M, Gustavson KH, Pettersson U. Wadelius C, et al. Among authors: pettersson u. Scand J Clin Lab Invest. 1991 Nov;51(7):625-33. doi: 10.1080/00365519109104573. Scand J Clin Lab Invest. 1991. PMID: 1810022

8

Galactosemia caused by a point mutation that activates cryptic donor splice site in the galactose-1-phosphate uridyltransferase gene.

Wadelius C, Lagerkvist A, Molin AK, Larsson A, von Döbeln U, Pettersson U. Wadelius C, et al. Among authors: pettersson u. Genomics. 1993 Aug;17(2):525-6. doi: 10.1006/geno.1993.1363. Genomics. 1993. PMID: 8406510 No abstract available.

9

[Molecular genetic diagnostics--experiences from Uppsala].

Annerén G, Dahl N, Gustavson KH, Pettersson U, Wadelius C. Annerén G, et al. Among authors: pettersson u. Lakartidningen. 1988 Jun 15;85(24):2186, 2188, 2191-2. Lakartidningen. 1988. PMID: 3290601 Swedish. No abstract available.

10

Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene.

Steén-Bondeson ML, Dahl N, Tönnesen T, Kleijer WJ, Seidlitz G, Gustavson KH, Wilson PJ, Morris CP, Hopwood JJ, Pettersson U. Steén-Bondeson ML, et al. Among authors: pettersson u. Hum Mol Genet. 1992 Jun;1(3):195-8. doi: 10.1093/hmg/1.3.195. Hum Mol Genet. 1992. PMID: 1303177

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